Human Phenotype Ontology 
Grandparent Node:
expand
Syndactyly (HP:0001159)help
Parent Node:
expand
Finger syndactyly (HP:0006101)help
..Starting node
..expand
4-5 finger syndactyly (HP:0010705)help
Term ID: 10705
Name: 4-5 finger syndactyly
Synonym: Webbed 4th-5th finger
Definition: Syndactyly with fusion of fingers four and five.
Comments:
Reference: HP:0010705
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expand1-2 finger syndactyly (HP:0010704) help
..expand1-3 finger syndactyly (HP:0010706) help
..expand1-4 finger syndactyly (HP:0010707) help
..expand1-5 finger syndactyly (HP:0010708) help
..expand2-3 finger syndactyly (HP:0001233) help
..expand2-4 finger syndactyly (HP:0010709) help
..expand2-5 finger syndactyly (HP:0010692) help
..expand3-4 finger syndactyly (HP:0006097) help
..expand3-5 finger syndactyly (HP:0010710) help
..expandCutaneous finger syndactyly (HP:0010554) help
..expandOsseous finger syndactyly (HP:0010492) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0010705HP:00107054-5 finger syndactyly0GJA1 CL E G H2697164200Oculodentodigital dysplasia164200C0812437OMIM11091414274121014
HP:0010705HP:00107054-5 finger syndactyly0GJA1 CL E G H2697257850Oculodentodigital dysplasia, autosomal recessive257850C2749477OMIM11091414274121014
HP:0010705HP:00107054-5 finger syndactyly0GJA1 CL E G H2697186100Syndactyly type 3186100C1861366OMIM11091414274121014
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :GJA1

Diseases (3) :164200 257850 186100
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.